Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
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Seite 211
... blood were available . In 1973 , it was reported that fetal blood could be obtained by umbilical cord puncture under direct visualization . In the 3 cases studied , no free bleeding was observed , although a hematoma was found in one ...
... blood were available . In 1973 , it was reported that fetal blood could be obtained by umbilical cord puncture under direct visualization . In the 3 cases studied , no free bleeding was observed , although a hematoma was found in one ...
Seite 212
... blood stained . In each case , the hematocrit was less than 1 % and the average total volume of fetal blood lost in these cases was estimated to be approximately 1 ml . The authors suggest that the procedure was relatively simple and ...
... blood stained . In each case , the hematocrit was less than 1 % and the average total volume of fetal blood lost in these cases was estimated to be approximately 1 ml . The authors suggest that the procedure was relatively simple and ...
Seite 273
... blood group Rodgers blood group 06p210 - p220 Ir 14685 df T 06p210 - p220 MLR - 2 15786 dp Р immune response iocus ( or loci ) mixed lymphocyte reaction , weak 06p210 - p220 MLR - S 15786 df C mixed lymphocyte reaction 06p Pg 16970 df C ...
... blood group Rodgers blood group 06p210 - p220 Ir 14685 df T 06p210 - p220 MLR - 2 15786 dp Р immune response iocus ( or loci ) mixed lymphocyte reaction , weak 06p210 - p220 MLR - S 15786 df C mixed lymphocyte reaction 06p Pg 16970 df C ...
Inhalt
The legal aspects of genetic screening and counseling | 3 |
Some trends in the study of spontaneous and induced mutation in | 19 |
Temporal genes and developmental programs | 33 |
Urheberrecht | |
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aberrations Acad activity alleles Amer amniocentesis amniotic fluid amniotic fluid cells analysis antenatal antigens assay autosomal banding biochemical blood group Bodmer cancer cell hybridization chromatid chromosome abnormalities clinical clones congenital correlation culture cytogenetic deficiency detected determined differentiation disease disorders donor Down's syndrome Editors environmental enzyme errors of metabolism extinction factors fetal fetus fibroblasts frequency functions Galjaard gene genetic distance genome H-2 complex hemoglobin HLA-D Human Genetics inborn errors individuals inheritance involved karyotype lactose Lancet linkage disequilibrium loci locus lymphocytes malformations marker maternal methods microcell Milunsky mouse mutagens mutation rates Nature Lond neural tube defects newborns normal observed parents patients phenotype phenylketonuria polymorphism population genetics possible pregnancies prenatal diagnosis Press Proc protein recent risk Ruddle samples selection somatic cell specific structural studies suggested Table techniques tissue translocation tumors variants X chromosome Zinkernagel